BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 10930359)

  • 1. A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21.
    Cohn DH; Shohat T; Yahav M; Ilan T; Rechavi G; King L; Shohat M
    Am J Hum Genet; 2000 Sep; 67(3):647-51. PubMed ID: 10930359
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and genetic characterization of an autosomal dominant nephropathy.
    Parvari R; Shnaider A; Basok A; Katchko L; Borochovich Z; Kanis A; Landau D
    Am J Med Genet; 2001 Mar; 99(3):204-9. PubMed ID: 11241491
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial juvenile hyperuricemic nephropathy: localization of the gene on chromosome 16p11.2-and evidence for genetic heterogeneity.
    Stibůrková B; Majewski J; Sebesta I; Zhang W; Ott J; Kmoch S
    Am J Hum Genet; 2000 Jun; 66(6):1989-94. PubMed ID: 10780922
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.
    Cuisset L; Drenth JP; Berthelot JM; Meyrier A; Vaudour G; Watts RA; Scott DG; Nicholls A; Pavek S; Vasseur C; Beckmann JS; Delpech M; Grateau G
    Am J Hum Genet; 1999 Oct; 65(4):1054-9. PubMed ID: 10486324
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new locus on chromosome 12p13.3 for pseudohypoaldosteronism type II, an autosomal dominant form of hypertension.
    Disse-Nicodème S; Achard JM; Desitter I; Houot AM; Fournier A; Corvol P; Jeunemaitre X
    Am J Hum Genet; 2000 Aug; 67(2):302-10. PubMed ID: 10869238
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21.
    Zhang XJ; Gao M; Li M; Li M; Li CR; Cui Y; He PP; Xu SJ; Xiong XY; Wang ZX; Yuan WT; Yang S; Huang W
    J Invest Dermatol; 2003 May; 120(5):776-80. PubMed ID: 12713580
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.
    Bouhouche A; Benomar A; Birouk N; Mularoni A; Meggouh F; Tassin J; Grid D; Vandenberghe A; Yahyaoui M; Chkili T; Brice A; LeGuern E
    Am J Hum Genet; 1999 Sep; 65(3):722-7. PubMed ID: 10441578
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.
    Feather SA; Malcolm S; Woolf AS; Wright V; Blaydon D; Reid CJ; Flinter FA; Proesmans W; Devriendt K; Carter J; Warwicker P; Goodship TH; Goodship JA
    Am J Hum Genet; 2000 Apr; 66(4):1420-5. PubMed ID: 10739767
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.
    Kumar S; Deffenbacher K; Marres HA; Cremers CW; Kimberling WJ
    Am J Hum Genet; 2000 May; 66(5):1715-20. PubMed ID: 10762556
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.
    Fontaine B; Davoine CS; Dürr A; Paternotte C; Feki I; Weissenbach J; Hazan J; Brice A
    Am J Hum Genet; 2000 Feb; 66(2):702-7. PubMed ID: 10677329
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.
    Morlé L; Bozon M; Zech JC; Alloisio N; Raas-Rothschild A; Philippe C; Lambert JC; Godet J; Plauchu H; Edery P
    Am J Hum Genet; 2000 Dec; 67(6):1592-7. PubMed ID: 11035633
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.
    Hand CK; Khoris J; Salachas F; Gros-Louis F; Lopes AA; Mayeux-Portas V; Brewer CG; Brown RH; Meininger V; Camu W; Rouleau GA
    Am J Hum Genet; 2002 Jan; 70(1):251-6. PubMed ID: 11706389
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.
    Valente EM; Bentivoglio AR; Dixon PH; Ferraris A; Ialongo T; Frontali M; Albanese A; Wood NW
    Am J Hum Genet; 2001 Apr; 68(4):895-900. PubMed ID: 11254447
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.
    Hart TC; Gorry MC; Hart PS; Woodard AS; Shihabi Z; Sandhu J; Shirts B; Xu L; Zhu H; Barmada MM; Bleyer AJ
    J Med Genet; 2002 Dec; 39(12):882-92. PubMed ID: 12471200
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.
    Laing NG; Majda BT; Akkari PA; Layton MG; Mulley JC; Phillips H; Haan EA; White SJ; Beggs AH; Kunkel LM
    Am J Hum Genet; 1992 Mar; 50(3):576-83. PubMed ID: 1347195
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Confirmation of linkage to 1q21-31 in a Danish autosomal dominant juvenile-onset glaucoma family and evidence of genetic heterogeneity.
    Graff C; Urbak SF; Jerndal T; Wadelius C
    Hum Genet; 1995 Sep; 96(3):285-9. PubMed ID: 7649543
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of a locus on chromosome 1q44 for familial cold urticaria.
    Hoffman HM; Wright FA; Broide DH; Wanderer AA; Kolodner RD
    Am J Hum Genet; 2000 May; 66(5):1693-8. PubMed ID: 10741953
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic and physical mapping of the locus for autosomal dominant renal Fanconi syndrome, on chromosome 15q15.3.
    Lichter-Konecki U; Broman KW; Blau EB; Konecki DS
    Am J Hum Genet; 2001 Jan; 68(1):264-8. PubMed ID: 11090339
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1.
    Xu SY; Schwartz M; Rosenberg T; Gal A
    Hum Mol Genet; 1996 Aug; 5(8):1193-7. PubMed ID: 8842740
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16.
    Sylvius N; Tesson F; Gayet C; Charron P; Bénaïche A; Peuchmaurd M; Duboscq-Bidot L; Feingold J; Beckmann JS; Bouchier C; Komajda M
    Am J Hum Genet; 2001 Jan; 68(1):241-6. PubMed ID: 11085912
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.